为生活挑战量身定制的实际和情感同伴支持:退伍军人健康管理局妇女诊所的进步个性化支持随机临床试点试验。

Emily M Johnson, Ellen Poleshuck, Kyle Possemato, Brittany Hampton, Jennifer S Funderburk, Harminder Grewal, Catherine Cerulli, Marsha Wittink
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引用次数: 0

摘要

简介女性退伍军人经历了广泛的压力源(如家庭、关系和经济)以及高比率的心理健康和身体健康状况,所有这些都会导致高水平的压力。个性化进步支持(PSP)是一种基于证据的干预措施,非常适合支持压力大的女性退伍军人,因为它涉及卡片分类任务,以优先考虑问题,以及务实和情感支持,以制定和实施解决这些问题的个性化计划。我们的目标是探索交付的人群和背景,并评估其可行性、可接受性和,以及同行专家提供的PSP对退伍军人健康管理局(VHA)妇女健康中心现有服务的补充作用。材料和方法该随机对照试点试验将照常治疗加PSP与照常治疗进行了比较,并使用先验的Go/No-Go标准来确定每种结果的成功率。我们就VHA妇女健康中心的人口和分娩环境采访了工作人员,并使用快速定性方法分析了采访。为了进行快速定性分析,我们创建了每个访谈的模板摘要,以确定每个先验主题中的关键概念,审查了所有访谈中每个主题的内容,并最终审查了各个主题中的重要概念。我们使用招聘率和保留率评估了可行性;通过老兵满意度、与同事的工作关系和员工满意度的可接受性;以及基于经历了结果(如压力、心理健康症状和生活质量)重大变化的退伍军人比例的效用。弗吉尼亚州锡拉丘兹人类受试者机构审查委员会批准了所有程序。结果工作人员访谈强调,女性退伍军人有许多未得到满足的社会需求和女性共同关心的问题,这增加了她们护理的复杂性;呼吁与医疗团队中的某个人建立支持、一致、信任的关系;并且需要许多资源(例如,社会工作者等工作人员、法律支持等服务以及尿布等实物)来支持他们的需求(其中一些资源在VHA中可用,但可能需要人员配置或访问支持,而其中一些资源不可用)。可行性结果表明,在进行更大规模的试验之前,需要修改PSP和研究方法,以提高干预和评估保留率;试验结束时,招募率是可以接受的。PSP的老兵接受度很高。退伍军人的结果表明,有希望改善女性退伍军人的压力、心理健康症状和生活质量。结论鉴于效用的可接受性和有希望的结果,有必要对设计进行修改,以提高不符合先验Go/No-Go标准的可行性结果。这些结果支持未来在VHA妇女健康中心进行PSP试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Practical and Emotional Peer Support Tailored for Life's Challenges: Personalized Support for Progress Randomized Clinical Pilot Trial in a Veterans Health Administration Women's Clinic.

Introduction: Women Veterans experience a broad range of stressors (e.g., family, relationship, and financial) and high rates of mental health and physical health conditions, all of which contribute to high levels of stress. Personalized Support for Progress (PSP), an evidence-based intervention, is well suited to support women Veterans with high stress as it involves a card-sort task to prioritize concerns as well as pragmatic and emotional support to develop and implement a personalized plan addressing those concerns. Our aims were to explore the population and context for delivery and evaluate the feasibility, acceptability, and utility of PSP delivered by a peer specialist to complement existing services in a Veterans Health Administration (VHA) Women's Wellness Center.

Materials and methods: This randomized controlled pilot trial compared treatment as usual plus PSP to treatment as usual and used the a priori Go/No-Go criteria to establish success for each outcome. We interviewed staff regarding the population and delivery context at a VHA Women's Wellness Center and analyzed interviews using a rapid qualitative approach. For the rapid qualitative analysis, we created templated summaries of each interview to identify key concepts within each a priori theme, reviewed each theme's content across all interviews, and finally reviewed key concepts across themes. We evaluated feasibility using recruitment and retention rates; acceptability via Veteran satisfaction, working relationship with the peer, and staff satisfaction; and utility based on the proportion of Veterans who experienced a large change in outcomes (e.g., stress, mental health symptoms, and quality of life). The Syracuse VA Human Subjects Institutional Review Board approved all procedures.

Results: Staff interviews highlight that women Veterans have numerous unmet social needs and concerns common among women which increase the complexity of their care; call for a supportive, consistent, trusting relationship with someone on their health care team; and require many resources (e.g., staff such as social workers, services such as legal support, and physical items such as diapers) to support their needs (some of which are available within VHA but may need support for staffing or access, and some of which are unavailable). Feasibility outcomes suggest a need to modify PSP and research methods to enhance intervention and assessment retention before the larger trial; the recruitment rate was acceptable by the end of the trial. Veteran acceptability of PSP was high. Veteran outcomes demonstrate promise for utility to improve stress, mental health symptoms, and quality of life for women Veterans.

Conclusions: Given the high acceptability and promising outcomes for utility, changes to the design to enhance the feasibility outcomes which failed to meet the a priori Go/No-Go criteria are warranted. These outcomes support future trials of PSP within VHA Women's Wellness Centers.

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